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通过流式细胞术分离小鼠胚胎神经干细胞并鉴定神经干细胞标志物。

Isolation of Mouse Embryonic Neural Stem Cells and Characterization of Neural Stem Markers by Flow Cytometry.

机构信息

Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, ON, Canada.

Lady Davis Institute for Medical Research, Jewish General Hospital, Chemin de la Côte-Sainte-Catherine, Montreal, QC, Canada.

出版信息

Methods Mol Biol. 2022;2515:297-308. doi: 10.1007/978-1-0716-2409-8_18.

Abstract

Neurogenesis is outlined as a process in which new neurons are generated from neural stem cells (NSCs). This process comprises proliferation and fate specification of NSCs, migration of newborn neurons, and their maturation. Defects in embryonic neurogenesis have emerged as a key mechanism underlying neurodevelopmental disorders such as autism spectrum disorders and intellectual disability. An impairment in neurogenesis has also been observed in neurodegenerative disorders such as Huntington's disease. Transgenic animal models of neurodevelopmental and neurodegenerative diseases have been developed which serve as invaluable tools to investigate the early mechanisms of disease pathogenesis. In this chapter, we describe our optimized method to obtain and maintain reproducible neurosphere cultures from transgenic or patient mouse models followed by characterization of NSCs by flow cytometry.

摘要

神经发生被描述为一种新神经元从神经干细胞(NSCs)中产生的过程。这个过程包括 NSCs 的增殖和命运特化、新生神经元的迁移及其成熟。胚胎神经发生缺陷已成为自闭症谱系障碍和智力障碍等神经发育障碍的关键机制。神经退行性疾病,如亨廷顿病,也观察到神经发生受损。神经发育和神经退行性疾病的转基因动物模型已经开发出来,这些模型是研究疾病发病机制早期机制的宝贵工具。在这一章中,我们描述了一种从转基因或患者小鼠模型中获得和维持可重复神经球培养的优化方法,然后通过流式细胞术对 NSCs 进行特征分析。

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